Application · Mass Spectrometry Imaging

Lipid Imaging: Drawing the 'Lipid Map' on Tissue Sections

Lipids are both structural components of cell membranes and signaling molecules and energy reserves. The distribution differences of different lipids in tissue are often associated with physiological state and disease. Lipid imaging uses MSI to present in-situ the spatial distribution of various lipids (PC, PE, SM, cholesterol, GalCer, etc.) on sections, allowing researchers to directly see 'which lipid is enriched in which region'.
Table of Contents
1. Why Lipid Imaging Is So Important2. Technical Advantages of DPI in Lipid Imaging3. Connection with Pathology and Neuroscience4. Resolution and Multi-Omics Integration
Schematic principle: ion source ionizes the sample spot-by-spot Tissue section Sample Ionization beam Lipid Imaging: Drawing the 'Lipid Map' on Tissue Sections Ions MS analyzer
Lipid Imaging: Drawing the 'Lipid Map' on Tissue Sections — schematic diagram

1. Why Lipid Imaging Is So Important

The lipid family is large, with similar structures but very different functions. Taking the DPI case as an example, positive ion mode can present choline, phosphocholine, PC, SM, cholesterol and various neutral GalCer lipids; negative ion mode can present PE, PE-O, PS, PI, ST, etc. The spatial distribution of different lipids directly reflects membrane structure, signaling state and metabolic activity.

It is especially valuable in neuroscience and tumor research: mouse brain sections can simultaneously image neurotransmitters and various lipids; in the melanocytic nevus case, the nevus region and normal tissue showed systematic differences in non-polar lipids such as MAG/DAG/TG and in S1P, cholesterol, PC and SM.

2. Technical Advantages of DPI in Lipid Imaging

Lipids span a wide polarity range, from strongly polar phospholipids to completely non-polar triglycerides and cholesterol. Traditional DESI has polarity bias against non-polar components and strong ion suppression; the Neo-Source MSI DPI, through desorption electrospray ionization combined with photochemical post-ionization, has no polarity bias, simultaneously covering polar and non-polar lipids, with overall metabolite signal enhanced by 1–3 orders of magnitude.

Published quantitative cases show that cholesterol signal in mouse brain increased by about 205x; in negative ion mode PE-O/PE signal increased by 2–4x, intuitively reflecting the sensitivity leap of photoionization for lipids.

3. Connection with Pathology and Neuroscience

Lipid distribution can be registered with pathological structures: in the DPI melanocytic nevus study, the specific distributions of S1P, cholesterol, PC34:1 and PC38:4 highly matched the H&E nevus region and cholesterol aggregation in the nevus was verified by IHC (Talanta, 2021). In the neuroscience direction, neurotransmitter and lipid co-imaging provides molecular spatial evidence for neurochemistry and pharmacological research.

Matrix-free preparation makes such lipid studies, which often require many sample comparisons, easier to deploy: the two Neo-Source imaging sources are matrix-free and measure on demand, and the section remains intact after imaging for continued H&E or IHC validation.

4. Resolution and Multi-Omics Integration

DPI's 20–200 μm resolution can depict lipid partitions of organs and local lesions; to enter single-cell/subcellular scale, the Neo-Source MSI LDPI provides 2–3 μm matrix-free ambient imaging as a supplement.

DPI is engineered to be compatible with mainstream mass spectrometers from Agilent, AB SCIEX and Thermo. It provides a self-developed titanium-alloy ion transfer tube that does not damage the sample at the front end and is detachable for cleaning, enabling stable and reproducible lipid imaging, and it can be combined with spatial metabolomics and spatial proteomics for multi-omics integration.

Frequently Asked Questions (FAQ)

Can lipid imaging distinguish structurally similar lipids?
MSI distinguishes lipid types based on mass-to-charge ratio (m/z) and can simultaneously present the different spatial distributions of PC, PE, SM, cholesterol, GalCer and many other lipids on sections.
How to read the lipid sensitivity improvement data of DPI?
Cholesterol signal in mouse brain increased by about 205x and negative-ion PE-O/PE by 2–4x, reflecting the sensitivity enhancement of photoionization for lipids, not indicating the true concentration changed by that much.
Why does lipid imaging value no polarity bias?
Because lipids span a wide polarity range, from strongly polar phospholipids to non-polar triglycerides/cholesterol; DPI's photochemical post-ionization has no polarity bias and covers them simultaneously.
What is the use of LDPI at 2–3 μm for lipid imaging?
Higher resolution can judge whether lipids localize to specific organelles or cell bands, entering single-cell/subcellular scale.

Get Specifications & Quotation

To obtain detailed specifications, compatible models, or a quotation for the MSI LDPI / DPI full series imaging ion sources, visit the Neo-Source official website, or contact the official team for compatibility advice tailored to your mass spectrometer (Agilent / SCIEX / Thermo and other mainstream MS).

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